Open Access

Table C.2

continued.

Molecule Transition Frequency (MHz) Eup(K) Aij (s−1) Receiver RMS (K)x) Positions
CH3OH-A 22−31 335133.570(13) 44.7 2.69 × 10−5 L* 0.037 -
NHD2 11,1,1 − 00,0,1 335446.321(3) 16.3 1.47 × 10−5 L 0.076 E
NHD2 11,1,0 − 00,0,0 335513.793(3) 16.1 1.29 × 10−5 L 0.082 E
CH3OH-A+ 71 − 61 335582.017(5) 79.0 1.63 × 10−4 L* 0.040 -
CH3OH-A−+ 121 − 120 336865.149(12) 197.1 4.07 × 10−4 L* 0.037 -
C17O 3−2 337061.214(2) 32.4 1.81 × 10−6 L 0.033 A/B, E, E1, E2, W1, W2, HE2
CH3OH-E 33−42 337135.853(14) 61.6 1.58 × 10−5 L* 0.037 -
C34S 7−6 337396.459(1) 64.8 8.00 × 10−4 L 0.054 A/B
H2CS 101,10−91,9 338083.195(50) 102.4 0.58 × 10−3 L 0.047 A/B
CH3OH-E 70−60 338124.488(5) 78.1 1.70 × 10−4 L 0.061 A/B, E1, HE2
SO2 184,14 − 183,15 338305.993(1) 196.8 3.27 × 10−4 L 0.058 A/B
CH3OH-E 7−1−6-1 338344.588(5) 70.6 1.67 × 10−4 L 0.054 A/B, E1, E2, W2, HE2
CH3OH-A+ 70−60 338408.698(5) 65.0 1.70 × 10−4 L 0.044 A/B, E1, E2, W2, HE2
CH3OH-E f) 7−4−6−4 338504.065(5) 152.9 1.15 × 10−4 L* 0.036 -
CH3OH-A−f) 74−64 338512.632(5) 145.3 1.15 × 10−4 L* 0.036 -
CH3OH-A+f) 74−64 338512.644(5) 145.3 1.15 × 10−4 L* 0.036 -
CH3OH-A−f) 72−62 338512.853(5) 102.7 1.57 × 10−4 L* 0.036 -
CH3OH-A+g) 73−63 338540.826(5) 114.8 1.39 × 10−4 L* 0.036 -
CH3OH-A−g) 73−63 338543.152(5) 114.8 1.39 × 10−4 L* 0.036 -
CH3OH-E 7−3−6−3 338559.963(5) 127.7 1.40 × 10−4 L* 0.036 -
CH3OH-E 73−63 338583.216(5) 112.7 1.39 × 10−4 L* 0.036 -
CH3OH-E 71−61 338614.936(5) 86.1 1.71 × 10−4 L* 0.034 -
CH3OH-A+ 72−62 338639.802(5) 102.7 1.58 × 10−4 L* 0.034 -
CH3OH-Eh) 72−62 338721.693(5) 87.3 1.55 × 10−4 L 0.039 A/B, E1
CH3OH-Eh) 7−2−6−2 338722.898(5) 90.9 1.57 × 10−4 L 0.039 A/B, E1
SO 33−23 339341.459(70) 25.5 1.45 × 10−5 L 0.047 A/B, E, E1, E2, W2
34SO 89−78 339857.269(14) 77.3 5.08 × 10−4 L 0.048 A/B
CN 35/2,7/2−23/2,5/2 340031.549(3) 32.6 3.85 × 10−4 L 0.036 A/B, E, E1
CN 35/2,5/2−23/2,3/2 340035.408(50) 32.6 3.23 × 10−4 L 0.043 A/B, E, HE2
C33S 70−60 340052.575(0) 65.3 0.82 × 10−3 L 0.071 A/B
CH3OH-A+ 22−31 340141.143(13) 44.7 2.78 × 10−5 L* 0.059 -
CNi) 37/2,9/2−25/2,7/2 340247.770(50) 32.7 4.13 × 10−4 L 0.064 A/B, E, E1, HE2
CNi) 37/2,5/2−25/2,3/2 340248.544(4) 32.7 3.67 × 10−4 L 0.064 A/B, E, E1, HE2
CH3OH-A−+ 131−130 342729.796(13) 227.5 4.23 × 10−4 L* 0.054 -
CS 7−6 342882.850(5) 65.8 8.39 × 10−4 L 0.092 A/B, E1, W1
SO 88−77 344310.612(70) 87.5 5.19 × 10−4 L 0.006 A/B, E1, W1
SO2j) 132,12−121,11 345338.538(2) 93.0 2.38 × 10−4 L* 0.041 A/B
H13 CNj) 4−3 345339.769(1) 41.4 1.90 × 10−3 L 0.041 A/B
CO 3−2 345795.990(1) 33.2 2.50 × 10−6 L 0.046 A/B, E, E1, E2, W1, W2, HE2
CH3OH-A−k) 54−63 346202.719(15) 115.2 2.18 × 10−5 L* 0.038 -
CH3OH-A+k) 54−63 346204.271(15) 115.2 2.18 × 10−5 L* 0.038 -
SO 89−78 346528.481(70) 78.8 5.38 × 10−4 L 0.084 A/B, E1, W1, W2
SO2 191,19−180,18 346652.169(1) 168.1 5.22 × 10−4 L 0.074 A/B
H13CO+ 4−3 346998.344(12) 41.6 3.29 × 10−3 L 0.013 A/B, E, E1, HE2
SiO 8−7 347330.581(7) 75.0 2.20 × 10−3 L 0.011 A/B, E1
H2CS 101,9−91,8 348534.365(50) 105.2 0.63 × 10−3 L 0.031 A/B
C2H 49/2,4−37/2,3 349337.706(22) 41.9 1.31 × 10−4 L 0.012 A/B, E1
C2H 47/2,3−35/2,2 349399.276(21) 41.9 1.25 × 10−4 L 0.012 A/B, E1
CH3OH-El) 40−3−1 350687.662(13) 36.3 8.67 × 10−5 L 0.048 A/B, E, E1, E2, W2, HE2
NO l) 4−,7/2,9/2−3+,5/2,7/2 350689.494(20) 36.1 5.42 × 10−6 L 0.053 A/B, E, E1, HE2
NO l) 4−,7/2,7/2−3+,5/2,5/2 350690.766(20) 36.1 4.98 × 10−6 L 0.053 A/B, E, HE2
CH3OH-A+ 11−00 350905.100(11) 16.8 3.32 × 10−4 L 0.054 A/B, E, E1, E2, W2, HE2
NO 4+,7/2,9/2−3−,5/2,7/2 351043.524(10) 36.1 5.43 × 10−6 L 0.040 A/B, E, E1, HE2
NO 4+,7/2,7/2−3−,5/2,5/2 351051.705(10) 36.1 4.99 × 10−6 L 0.040 A/B, E, E1, HE2
SO2 53,3 − 42,2 351257.223(2) 35.9 3.36 × 10−4 L 0.059 A/B, E1

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